1. An audit of familial juvenile polyposis at the Tel Aviv Medical Center: demographic, genetic and clinical features

   • Paul Rozen
   • Ziona Samuel
   • Zamir Halpern

   OriginalPaper Pages: 1 - 7

2. The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours

   • Astrid T. Stormorken
   • Wolfram Müller
   • Pål Møller

   OriginalPaper Pages: 9 - 13

3. Does the occurrence of certain rare cancers indicate an inherited cancer susceptibility?

   • Sara Levene
   • Gillian Scott
   • Shirley Hodgson

   OriginalPaper Pages: 15 - 25

4. Quality of life in patients with multiple endocrine neoplasia type 1 (MEN1)

   • G. Berglund
   • A. Lidén
   • K. Nordin

   OriginalPaper Pages: 27 - 33

5. The effect of disease penetrance, family size, and age of onset on family history with application to setting eligibility criteria for genetic testing

   • Alexandre Sibert
   • David E. Goldgar

   OriginalPaper Pages: 35 - 42

6. Attenuated familial adenomatous polyposis (AFAP): a review of the literature

   • Anne Lyster Knudsen
   • Marie Luise Bisgaard
   • Steffen Bülow

   ReviewPaper Pages: 43 - 55

7. Genetic susceptibility to prostate cancer: a review

   • Bas A. J. Verhage
   • Lambertus A. L. M. Kiemeney

   ReviewPaper Pages: 57 - 67

8. Instructions for authors

   Instructions for Authors Pages: 69 - 71